ICON is at the forefront of clinical research and development, driving innovation in partnership with global pharmaceutical companies. Their focus on diversity, inclusion, and belonging fosters an empowering environment, where employees are encouraged to perform at their best and make a positive impact on saving lives.
Key Responsibilities
As a Clinical Research Associate, you will manage multiple aspects of clinical trials, ensuring smooth operations across sites. Key duties include:
- On-Site Monitoring: Conduct site visits to ensure compliance with protocols and regulations.
- IRB Submissions: Handle Institutional Review Board submissions efficiently.
- Site Management: Manage communication and activities for assigned sites.
- Stakeholder & Vendor Coordination: Engage with multiple stakeholders to maintain timelines and resolve issues.
Qualifications
- Educational Requirements:
- B.Pharm/M.Pharm/Pharm D/BDS/MBBS
- Experience:
- Minimum 3 years of onsite monitoring experience (beyond training) in Oncology studies.
- Additional Skills:
- Experience with AZ Oncology processes.
- Strong communication skills to manage cross-functional teams.
Preferred Locations: Mumbai, Delhi
